Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 13 |
NetGPI | no | yes: 0, no: 13 |
Related structures:
AlphaFold database: E9ARB9
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 2 |
GO:0003924 | GTPase activity | 7 | 2 |
GO:0003925 | G protein activity | 2 | 2 |
GO:0016462 | pyrophosphatase activity | 5 | 2 |
GO:0016787 | hydrolase activity | 2 | 2 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 2 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 2 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 2 |
GO:0098772 | molecular function regulator activity | 1 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 100 | 104 | PF00656 | 0.716 |
CLV_C14_Caspase3-7 | 122 | 126 | PF00656 | 0.670 |
CLV_C14_Caspase3-7 | 252 | 256 | PF00656 | 0.291 |
CLV_NRD_NRD_1 | 248 | 250 | PF00675 | 0.393 |
CLV_NRD_NRD_1 | 78 | 80 | PF00675 | 0.493 |
CLV_NRD_NRD_1 | 88 | 90 | PF00675 | 0.550 |
CLV_PCSK_KEX2_1 | 248 | 250 | PF00082 | 0.393 |
CLV_PCSK_KEX2_1 | 78 | 80 | PF00082 | 0.493 |
CLV_PCSK_SKI1_1 | 14 | 18 | PF00082 | 0.504 |
CLV_PCSK_SKI1_1 | 284 | 288 | PF00082 | 0.322 |
CLV_PCSK_SKI1_1 | 315 | 319 | PF00082 | 0.300 |
CLV_PCSK_SKI1_1 | 368 | 372 | PF00082 | 0.377 |
CLV_PCSK_SKI1_1 | 409 | 413 | PF00082 | 0.416 |
CLV_PCSK_SKI1_1 | 477 | 481 | PF00082 | 0.389 |
CLV_PCSK_SKI1_1 | 93 | 97 | PF00082 | 0.693 |
DEG_MDM2_SWIB_1 | 38 | 46 | PF02201 | 0.348 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.499 |
DEG_ODPH_VHL_1 | 132 | 144 | PF01847 | 0.451 |
DEG_SPOP_SBC_1 | 119 | 123 | PF00917 | 0.688 |
DOC_CDC14_PxL_1 | 419 | 427 | PF14671 | 0.344 |
DOC_CKS1_1 | 345 | 350 | PF01111 | 0.387 |
DOC_CYCLIN_yClb1_LxF_4 | 1 | 7 | PF00134 | 0.481 |
DOC_MAPK_gen_1 | 281 | 290 | PF00069 | 0.373 |
DOC_MAPK_gen_1 | 409 | 419 | PF00069 | 0.459 |
DOC_MAPK_gen_1 | 474 | 481 | PF00069 | 0.398 |
DOC_MAPK_gen_1 | 89 | 97 | PF00069 | 0.716 |
DOC_MAPK_MEF2A_6 | 281 | 290 | PF00069 | 0.174 |
DOC_PP1_RVXF_1 | 157 | 163 | PF00149 | 0.300 |
DOC_PP1_RVXF_1 | 313 | 319 | PF00149 | 0.300 |
DOC_PP1_RVXF_1 | 91 | 98 | PF00149 | 0.659 |
DOC_PP2B_LxvP_1 | 49 | 52 | PF13499 | 0.389 |
DOC_PP4_FxxP_1 | 27 | 30 | PF00568 | 0.448 |
DOC_PP4_FxxP_1 | 449 | 452 | PF00568 | 0.356 |
DOC_USP7_MATH_1 | 109 | 113 | PF00917 | 0.714 |
DOC_USP7_MATH_1 | 135 | 139 | PF00917 | 0.581 |
DOC_USP7_MATH_1 | 222 | 226 | PF00917 | 0.421 |
DOC_WW_Pin1_4 | 107 | 112 | PF00397 | 0.668 |
DOC_WW_Pin1_4 | 344 | 349 | PF00397 | 0.386 |
DOC_WW_Pin1_4 | 402 | 407 | PF00397 | 0.510 |
DOC_WW_Pin1_4 | 84 | 89 | PF00397 | 0.647 |
LIG_14-3-3_CanoR_1 | 14 | 21 | PF00244 | 0.509 |
LIG_14-3-3_CanoR_1 | 150 | 154 | PF00244 | 0.306 |
LIG_14-3-3_CanoR_1 | 159 | 163 | PF00244 | 0.280 |
LIG_14-3-3_CanoR_1 | 248 | 258 | PF00244 | 0.369 |
LIG_14-3-3_CanoR_1 | 329 | 335 | PF00244 | 0.291 |
LIG_Actin_WH2_2 | 458 | 476 | PF00022 | 0.554 |
LIG_Actin_WH2_2 | 6 | 24 | PF00022 | 0.248 |
LIG_APCC_ABBA_1 | 164 | 169 | PF00400 | 0.342 |
LIG_BIR_III_2 | 106 | 110 | PF00653 | 0.578 |
LIG_BIR_III_4 | 374 | 378 | PF00653 | 0.389 |
LIG_BRCT_BRCA1_1 | 224 | 228 | PF00533 | 0.427 |
LIG_Clathr_ClatBox_1 | 287 | 291 | PF01394 | 0.257 |
LIG_deltaCOP1_diTrp_1 | 67 | 73 | PF00928 | 0.508 |
LIG_FHA_1 | 15 | 21 | PF00498 | 0.508 |
LIG_FHA_1 | 386 | 392 | PF00498 | 0.412 |
LIG_FHA_1 | 46 | 52 | PF00498 | 0.427 |
LIG_FHA_1 | 89 | 95 | PF00498 | 0.556 |
LIG_FHA_2 | 120 | 126 | PF00498 | 0.586 |
LIG_FHA_2 | 173 | 179 | PF00498 | 0.428 |
LIG_LIR_Apic_2 | 161 | 165 | PF02991 | 0.291 |
LIG_LIR_Apic_2 | 24 | 30 | PF02991 | 0.425 |
LIG_LIR_Gen_1 | 230 | 240 | PF02991 | 0.322 |
LIG_LIR_Gen_1 | 337 | 344 | PF02991 | 0.367 |
LIG_LIR_Gen_1 | 39 | 50 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 225 | 231 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 3 | 9 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 337 | 342 | PF02991 | 0.354 |
LIG_LIR_Nem_3 | 39 | 45 | PF02991 | 0.319 |
LIG_NRBOX | 293 | 299 | PF00104 | 0.427 |
LIG_PCNA_yPIPBox_3 | 289 | 302 | PF02747 | 0.334 |
LIG_Pex14_1 | 331 | 335 | PF04695 | 0.443 |
LIG_Pex14_1 | 40 | 44 | PF04695 | 0.441 |
LIG_Pex14_2 | 228 | 232 | PF04695 | 0.427 |
LIG_Pex14_2 | 318 | 322 | PF04695 | 0.352 |
LIG_Pex14_2 | 38 | 42 | PF04695 | 0.349 |
LIG_PTB_Apo_2 | 185 | 192 | PF02174 | 0.443 |
LIG_PTB_Phospho_1 | 185 | 191 | PF10480 | 0.334 |
LIG_SH2_NCK_1 | 183 | 187 | PF00017 | 0.238 |
LIG_SH2_PTP2 | 339 | 342 | PF00017 | 0.360 |
LIG_SH2_STAP1 | 140 | 144 | PF00017 | 0.300 |
LIG_SH2_STAP1 | 396 | 400 | PF00017 | 0.489 |
LIG_SH2_STAP1 | 466 | 470 | PF00017 | 0.388 |
LIG_SH2_STAT3 | 140 | 143 | PF00017 | 0.492 |
LIG_SH2_STAT5 | 309 | 312 | PF00017 | 0.312 |
LIG_SH2_STAT5 | 339 | 342 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 358 | 361 | PF00017 | 0.435 |
LIG_SH3_1 | 420 | 426 | PF00018 | 0.498 |
LIG_SH3_3 | 128 | 134 | PF00018 | 0.529 |
LIG_SH3_3 | 420 | 426 | PF00018 | 0.512 |
LIG_TRAF2_1 | 455 | 458 | PF00917 | 0.475 |
LIG_TRAF2_2 | 387 | 392 | PF00917 | 0.254 |
LIG_TYR_ITIM | 181 | 186 | PF00017 | 0.450 |
LIG_TYR_ITIM | 234 | 239 | PF00017 | 0.446 |
LIG_UBA3_1 | 246 | 254 | PF00899 | 0.174 |
MOD_CDC14_SPxK_1 | 87 | 90 | PF00782 | 0.531 |
MOD_CDK_SPK_2 | 84 | 89 | PF00069 | 0.554 |
MOD_CDK_SPxK_1 | 84 | 90 | PF00069 | 0.558 |
MOD_CDK_SPxxK_3 | 402 | 409 | PF00069 | 0.552 |
MOD_CK1_1 | 101 | 107 | PF00069 | 0.621 |
MOD_CK1_1 | 118 | 124 | PF00069 | 0.530 |
MOD_CK1_1 | 136 | 142 | PF00069 | 0.546 |
MOD_CK1_1 | 158 | 164 | PF00069 | 0.312 |
MOD_CK1_1 | 405 | 411 | PF00069 | 0.567 |
MOD_CK2_1 | 181 | 187 | PF00069 | 0.403 |
MOD_CK2_1 | 398 | 404 | PF00069 | 0.343 |
MOD_CK2_1 | 80 | 86 | PF00069 | 0.608 |
MOD_CK2_1 | 99 | 105 | PF00069 | 0.653 |
MOD_Cter_Amidation | 76 | 79 | PF01082 | 0.539 |
MOD_GlcNHglycan | 111 | 114 | PF01048 | 0.733 |
MOD_GlcNHglycan | 117 | 120 | PF01048 | 0.747 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.587 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.485 |
MOD_GlcNHglycan | 271 | 275 | PF01048 | 0.429 |
MOD_GlcNHglycan | 276 | 279 | PF01048 | 0.410 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.486 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.306 |
MOD_GSK3_1 | 398 | 405 | PF00069 | 0.550 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.655 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.641 |
MOD_N-GLC_1 | 351 | 356 | PF02516 | 0.358 |
MOD_NEK2_1 | 181 | 186 | PF00069 | 0.488 |
MOD_NEK2_1 | 351 | 356 | PF00069 | 0.344 |
MOD_NEK2_1 | 45 | 50 | PF00069 | 0.423 |
MOD_NEK2_1 | 80 | 85 | PF00069 | 0.580 |
MOD_NEK2_1 | 97 | 102 | PF00069 | 0.681 |
MOD_NEK2_2 | 427 | 432 | PF00069 | 0.606 |
MOD_PIKK_1 | 385 | 391 | PF00454 | 0.435 |
MOD_PKA_2 | 149 | 155 | PF00069 | 0.321 |
MOD_PKA_2 | 158 | 164 | PF00069 | 0.321 |
MOD_PKA_2 | 21 | 27 | PF00069 | 0.435 |
MOD_PKA_2 | 88 | 94 | PF00069 | 0.600 |
MOD_Plk_1 | 136 | 142 | PF00069 | 0.561 |
MOD_Plk_1 | 155 | 161 | PF00069 | 0.453 |
MOD_Plk_1 | 2 | 8 | PF00069 | 0.450 |
MOD_Plk_1 | 351 | 357 | PF00069 | 0.335 |
MOD_Plk_1 | 427 | 433 | PF00069 | 0.566 |
MOD_Plk_1 | 80 | 86 | PF00069 | 0.577 |
MOD_Plk_2-3 | 369 | 375 | PF00069 | 0.364 |
MOD_Plk_2-3 | 99 | 105 | PF00069 | 0.719 |
MOD_Plk_4 | 181 | 187 | PF00069 | 0.408 |
MOD_Plk_4 | 2 | 8 | PF00069 | 0.419 |
MOD_Plk_4 | 303 | 309 | PF00069 | 0.298 |
MOD_Plk_4 | 330 | 336 | PF00069 | 0.407 |
MOD_ProDKin_1 | 107 | 113 | PF00069 | 0.666 |
MOD_ProDKin_1 | 344 | 350 | PF00069 | 0.387 |
MOD_ProDKin_1 | 402 | 408 | PF00069 | 0.506 |
MOD_ProDKin_1 | 84 | 90 | PF00069 | 0.652 |
MOD_SUMO_rev_2 | 343 | 348 | PF00179 | 0.305 |
MOD_SUMO_rev_2 | 54 | 59 | PF00179 | 0.464 |
TRG_DiLeu_BaEn_1 | 230 | 235 | PF01217 | 0.291 |
TRG_DiLeu_BaEn_2 | 196 | 202 | PF01217 | 0.300 |
TRG_DiLeu_BaLyEn_6 | 312 | 317 | PF01217 | 0.285 |
TRG_ENDOCYTIC_2 | 183 | 186 | PF00928 | 0.476 |
TRG_ENDOCYTIC_2 | 236 | 239 | PF00928 | 0.365 |
TRG_ENDOCYTIC_2 | 244 | 247 | PF00928 | 0.315 |
TRG_ENDOCYTIC_2 | 339 | 342 | PF00928 | 0.360 |
TRG_ER_diArg_1 | 247 | 249 | PF00400 | 0.427 |
TRG_ER_diArg_1 | 78 | 80 | PF00400 | 0.505 |
TRG_NES_CRM1_1 | 362 | 374 | PF08389 | 0.386 |
TRG_Pf-PMV_PEXEL_1 | 14 | 19 | PF00026 | 0.506 |
TRG_Pf-PMV_PEXEL_1 | 249 | 253 | PF00026 | 0.410 |
TRG_Pf-PMV_PEXEL_1 | 78 | 82 | PF00026 | 0.594 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P848 | Leptomonas seymouri | 57% | 100% |
A0A0S4IV10 | Bodo saltans | 27% | 84% |
A0A1X0NSL3 | Trypanosomatidae | 32% | 92% |
A0A3S7WUR8 | Leishmania donovani | 91% | 100% |
A0A3S7X3S6 | Leishmania donovani | 25% | 100% |
A0A422NB36 | Trypanosoma rangeli | 34% | 99% |
A4H9A3 | Leishmania braziliensis | 79% | 100% |
A4HXM3 | Leishmania infantum | 91% | 100% |
A4I5W2 | Leishmania infantum | 25% | 100% |
C9ZPB8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 90% |
Q4QE44 | Leishmania major | 88% | 100% |
V5BEU9 | Trypanosoma cruzi | 32% | 97% |